Winter Linda E, Barenkamp Stephen J
Department of Pediatrics, St Louis University School of Medicine, Doisy Research Center, Saint Louis, MO 63104, USA.
Clin Vaccine Immunol. 2009 Jul;16(7):1040-6. doi: 10.1128/CVI.00090-09. Epub 2009 May 27.
The Hia autotransporter proteins are highly immunogenic surface adhesins expressed by nontypeable Haemophilus influenzae (NTHI). The objective of our study was to assess the opsonophagocytic activity of anti-Hia antibodies against homologous and heterologous NTHI. A segment of the hia gene that encodes a surface-exposed portion of the H. influenzae strain 11 Hia protein was cloned into a pGEMEX-2 expression vector. Escherichia coli JM101 was transformed with the resulting pGEMEX-Hia BstEII del recombinant plasmid, and recombinant fusion protein was recovered. An immune serum against recombinant GEMEX-Hia (rGEMEX-Hia)-mediated killing of the homologous NTHI strain 11 at a 1:160 titer and five heterologous Hia-expressing strains at titers of > or =1:40. Immune serum did not mediate killing of two Hia-knockout strains whose hia genes were inactivated but did mediate killing of one knockout strain at a high titer after the strain was transformed with a plasmid containing the hia gene. Immune serum did not mediate killing of HMW1/HMW2-expressing NTHI strains, which do not express the Hia adhesin. However, when two representative HMW1/HMW2-expressing strains were transformed with the plasmid containing the hia gene, they expressed abundant Hia and were susceptible to killing by the immune serum. Immune serum did not mediate killing of HMW1/HMW2-expressing strains transformed with the plasmid without the hia gene. Our results demonstrate that the Hia proteins of NTHI are targets of opsonophagocytic antibodies and that shared epitopes recognized by such antibodies are present on the Hia proteins of unrelated NTHI strains. These data argue for the continued investigation of the Hia proteins as vaccine candidates for the prevention of NTHI disease.
Hia自转运蛋白是不可分型流感嗜血杆菌(NTHI)表达的高度免疫原性表面黏附素。我们研究的目的是评估抗Hia抗体对同源和异源NTHI的调理吞噬活性。将编码流感嗜血杆菌11型Hia蛋白表面暴露部分的hia基因片段克隆到pGEMEX-2表达载体中。用所得的pGEMEX-Hia BstEII del重组质粒转化大肠杆菌JM101,并回收重组融合蛋白。抗重组GEMEX-Hia(rGEMEX-Hia)的免疫血清在效价为1:160时介导对同源NTHI菌株11的杀伤,在效价≥1:40时介导对5种异源表达Hia的菌株的杀伤。免疫血清不介导对两个hia基因失活的Hia敲除菌株的杀伤,但在一个敲除菌株用含hia基因的质粒转化后,免疫血清在高效价时介导对其的杀伤。免疫血清不介导对表达HMW1/HMW2而不表达Hia黏附素的NTHI菌株的杀伤。然而,当两个代表性的表达HMW1/HMW2的菌株用含hia基因的质粒转化后,它们表达大量Hia并易被免疫血清杀伤。免疫血清不介导对用不含hia基因的质粒转化的表达HMW1/HMW2的菌株的杀伤。我们的结果表明,NTHI的Hia蛋白是调理吞噬抗体的靶标,并且这些抗体识别的共同表位存在于不相关NTHI菌株的Hia蛋白上。这些数据支持继续研究将Hia蛋白作为预防NTHI疾病的候选疫苗。